Drug recall
Platelets Pheresis Leukocytes Reduced
FDA recall event 66106 · Class II · West Tennessee Regional Blood Center Inc
Key facts
| Event ID | 66106 |
|---|---|
| Recall numbers | B-2578-13 |
| Recalling firm | West Tennessee Regional Blood Center Inc |
| Product type | Biologics |
| Products | Platelets Pheresis Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, with no documentation of QC testing for platelet pH, was distributed. |
| Initiation date | Aug 8, 2013 |
| Report date | Sep 25, 2013 |
| Termination date | Sep 17, 2013 |
| City | Jackson |
| State | TN |
| Country | United States |
| FEI number | 1071200 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: